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1.
Reproduction ; 149(5): R219-27, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25628442

RESUMEN

Polycystic ovary syndrome (PCOS), a complex condition that affects women of reproductive age, is characterized by ovulatory dysfunction and androgen excess. Women with PCOS present higher prevalence of obesity, central adiposity, and dyslipidemia, and face increased risk of type 2 diabetes. PCOS is closely linked to functional derangements in adipose tissue. Adipocytes seem to be prone to hypertrophy when exposed to androgen excess, as experienced by women with PCOS, and both adipose tissue hypertrophy and hyperandrogenism are related to insulin resistance. Hypertrophic adipocytes are more susceptible to inflammation, apoptosis, fibrosis, and release of free fatty acids. Disturbed secretion of adipokines may also impact the pathophysiology of PCOS through their influence on metabolism and on sex steroid secretion. Chronic low-grade inflammation in PCOS is also related to hyperandrogenism and to the hypertrophy of adipocytes, causing compression phenomena in the stromal vessels, leading to adipose tissue hypoperfusion and altered secretion of cytokines. Lifestyle changes are the first-line intervention for reducing metabolic risks in PCOS and the addition of an insulin-sensitizing drug might be required. Nevertheless, there is not sufficient evidence in favor of any specific pharmacologic therapies to directly oppose inflammation. Further studies are warranted to identify an adipokine that could serve as an indirect marker of adipocyte production in PCOS, representing a reliable sign of metabolic alteration in this syndrome.


Asunto(s)
Adipoquinas/metabolismo , Tejido Adiposo/patología , Inflamación/etiología , Síndrome del Ovario Poliquístico/fisiopatología , Animales , Enfermedad Crónica , Femenino , Humanos , Inflamación/metabolismo , Inflamación/patología , Síndrome del Ovario Poliquístico/complicaciones
2.
Reprod Biol Endocrinol ; 11: 77, 2013 Aug 14.
Artículo en Inglés | MEDLINE | ID: mdl-23941060

RESUMEN

BACKGROUND: Polycystic ovary syndrome (PCOS) has been recognized as a metabolic disorder, manifested by abdominal obesity, insulin resistance, dyslipidemia and hypertension. Pigment epithelium-derived factor (PEDF), a member of the serine protease inhibitor family, is a pleiotropic protein known for its antiangiogenic, antioxidant, and neuroprotective properties and has been shown to induce insulin resistance and play a role in glucose metabolism. Recent studies investigating circulating PEDF levels show elevated serum PEDF in association with insulin resistance in normal-weight women with PCOS, but not in obese PCOS patients. The aims of this study were 1) to assess PEDF gene expression in subcutaneous adipose tissue (scAT) from women with PCOS and nonhirsute, ovulatory controls, and 2) to determine the circulating levels of PEDF in these groups. METHODS: Total RNA was extracted from adipose tissue biopsy samples and reverse-transcribed to cDNA. Real-time quantitative PCR was performed to determine relative gene expression levels. RESULTS: The 22 women with PCOS and 14 non-PCOS controls included in the study had similar age, BMI, and fasting glucose, triglycerides, and HDL-cholesterol levels. Participants with PCOS exhibited higher 2 h oral glucose tolerance test levels (p = 0.006), total (p = 0.026) and LDL-cholesterol (p = 0.036), Ferriman-Gallwey score (p = 0.003) and total testosterone (p = 0.001) as compared to controls. BMI-adjusted PEDF serum levels and scAT gene expression were similar in the PCOS and control groups (p = 0.622 and p = 0.509, respectively). Circulating PEDF levels were not associated with scAT PEDF gene expression. Multiple regression analysis revealed that, in women with PCOS, insulin contributed positively and significantly to serum PEDF (p = 0.027), independently of testosterone. CONCLUSION: Serum PEDF levels and scAT gene expression were associated with metabolic risk factors, but did not differ between women with PCOS and age- and BMI-matched controls. Circulating levels and scAT gene expression of PEDF were not associated in the study subjects, suggesting additional sources for PEDF in addition to or instead of fat tissue.


Asunto(s)
Proteínas del Ojo/metabolismo , Regulación de la Expresión Génica/fisiología , Factores de Crecimiento Nervioso/metabolismo , Síndrome del Ovario Poliquístico/metabolismo , Serpinas/metabolismo , Grasa Subcutánea/metabolismo , Adulto , Estudios de Casos y Controles , Proteínas del Ojo/sangre , Femenino , Regulación de la Expresión Génica/genética , Humanos , Factores de Crecimiento Nervioso/sangre , Serpinas/sangre , Adulto Joven
3.
Steroids ; 76(12): 1383-8, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21807013

RESUMEN

In polycystic ovary syndrome (PCOS), hypertension has been linked to androgen excess and insulin resistance. Aromatase, an enzyme encoded by the CYP19 gene, affects androgen metabolism and estrogen synthesis, influencing the androgen to estrogen balance. We characterized CYP19 gene expression in subcutaneous adipose tissue of women with PCOS and normal controls and evaluated the association between subcutaneous fat CYP19 mRNA, circulating hormone levels, and blood pressure. This case-control study was carried out with 31 PCOS patients and 27 BMI-matched normotensive non-hirsute women with regular cycles. Participants underwent anthropometric measurements, collection of blood samples, and adipose tissue biopsy (28 PCOS and 19 controls). Hypertension was defined as systolic blood pressure ≥ 130 mmHg and/or diastolic blood pressure ≥ 85 mmHg. PCOS patients were divided into normotensive and hypertensive. Main outcome measures were serum estrogen and androgen levels, estrogen-to-androgen ratio, and CYP19 gene expression in subcutaneous fat. Subcutaneous CYP19 mRNA was higher in hypertensive PCOS than in control and normotensive PCOS women (p = 0.014). Estrogen-to-androgen ratio was lower in hypertensive PCOS than controls (p < 0.003). Estrogen-to-androgen ratio ≤ 0.06 (median for the three groups) was observed in 91% of hypertensive PCOS women, vs. 37% and 61% in the control and normotensive PCOS groups (p = 0.011). CYP19 gene expression in subcutaneous fat of PCOS patient correlated positively with systolic (p = 0.006) and diastolic blood pressure (p = 0.009). Androgen excess and hyperinsulinemia may play a role in the molecular mechanisms that activate aromatase mRNA transcription in abdominal fat tissue.


Asunto(s)
Aromatasa/genética , Hipertensión/genética , Síndrome del Ovario Poliquístico/enzimología , Grasa Subcutánea/enzimología , Adulto , Andrógenos/sangre , Glucemia/análisis , Presión Sanguínea , Índice de Masa Corporal , Estudios de Casos y Controles , Estrógenos/sangre , Femenino , Expresión Génica , Humanos , Hiperinsulinismo/complicaciones , Hiperinsulinismo/enzimología , Hipertensión/etiología , Insulina/sangre , Síndrome del Ovario Poliquístico/complicaciones
4.
J Mol Histol ; 40(1): 53-8, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19199093

RESUMEN

Endometriosis is an estrogen-dependent disease, causing pelvic pain and infertility. c-fos is an early transcription factor that has been reported to be related to estradiol-dependent cell proliferation. The aim of the present study was to assess the c-fos gene and protein expression in pelvic endometriotic implants in comparison to normal endometrium from infertile women. An open, prospective and controlled study included 15 infertile women with endometriosis and 19 control infertile women. Endometrial and endometriotic biopsies were performed at the follicular phase and the samples were processed for RT-PCR and immunohistochemistry. ERalpha mRNA levels were similar in the endometriotic implants/eutopic endometrium from women with endometriosis and in normal tissue (P = 0.649). The aromatase gene, however, was not expressed in the eutopic endometrium from either control or endometriosis groups, and was only expressed in 50% of endometriotic implants (P = 0.044). c-fos gene expression was higher in endometriotic implants (1.32 +/- 0.13; P = 0.011) than in eutopic endometrium from patients with endometriosis (0.97 +/- 0.11) or from the control group (0.91 +/- 0.05). In addition, immunohistochemistry showed a more abundant distribution of c-Fos in the stroma of endometriotic tissue compared to eutopic endometrium. These data suggest that c-fos may play a role in the molecular mechanisms of estrogen action on the induction, promotion or progression of endometriosis.


Asunto(s)
Endometriosis/patología , Endometrio/patología , Proteínas Proto-Oncogénicas c-fos/genética , Adulto , Análisis de Varianza , Aromatasa/genética , Biomarcadores/análisis , Biopsia , Endometriosis/genética , Endometriosis/metabolismo , Endometrio/metabolismo , Receptor alfa de Estrógeno/genética , Estrógenos/metabolismo , Femenino , Expresión Génica , Humanos , Inmunohistoquímica , Pelvis , Proteínas Proto-Oncogénicas c-fos/biosíntesis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
5.
Parasitol. latinoam ; 58(3/4): 101-105, jul. 2003. ilus
Artículo en Inglés | LILACS | ID: lil-383486

RESUMEN

Tetratrichomonas didelphidis is a flagellated protozoan found in the intestine of opossums. The specimens were stained by the Giemsa method and by FLUTAX-2, an active fluorescent derivative of Taxol which binds to the ab-tubulin polimerized of microtubules of cells. Giemsa stain revealed the morphological features of trichomonads such as four anterior flagella, undulating membrane, axostyle and posterior flagellum. An intense fluorescence was observed in living trophozoites of T. didelphidis and Trichomonas vaginalis (used as control), incubated with FLUTAX-2. An analysis of the composition of the cytoskeleton of T. didelphidis will contribute to understanding the cellular morphology of the parasites. Key words: Tetratrichomonas didelphidis, microtubule cytoskeleton, fluorescent taxoid.


Asunto(s)
Animales , Citoesqueleto , Colorantes Fluorescentes , Técnicas In Vitro , Microtúbulos/ultraestructura , Trichomonas , Zarigüeyas , Trichomonas vaginalis
6.
Mem Inst Oswaldo Cruz ; 98(2): 273-6, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12764446

RESUMEN

Several diagnostic techniques have been employed for the detection of Trichomonas vaginalis. Microtubules constitute the cytoskeleton in eukaryotic cells and are sensitive to antimitotic drugs, such as Taxol (paclitaxel). We used FLUTAX a fluorescent taxoid - to analyze the microtubule distribution in living trophozoites of T. vaginalis in urine and in vaginal discharge. A high intensity of fluorescence was observed in living T. vaginalis, epithelial cells and leukocytes present in urine and vaginal discharge. Our preliminary results show the perspective of a new diagnostic technique for trichomonosis and will contribute to the understanding of the cytoskeleton of T. vaginalis.


Asunto(s)
Citoesqueleto/ultraestructura , Colorantes Fluorescentes , Paclitaxel/análogos & derivados , Taxoides , Vaginitis por Trichomonas/diagnóstico , Trichomonas vaginalis/ultraestructura , Animales , Centrosoma/ultraestructura , Femenino , Flagelos/ultraestructura , Humanos , Microscopía Fluorescente , Microtúbulos/ultraestructura , Excreción Vaginal/parasitología
7.
Mem. Inst. Oswaldo Cruz ; 98(2): 273-276, Mar. 15, 2003. ilus
Artículo en Inglés | LILACS | ID: lil-334267

RESUMEN

Several diagnostic techniques have been employed for the detection of Trichomonas vaginalis. Microtubules constitute the cytoskeleton in eukaryotic cells and are sensitive to antimitotic drugs, such as Taxol (paclitaxel). We used FLUTAX a fluorescent taxoid - to analyze the microtubule distribution in living trophozoites of T. vaginalis in urine and in vaginal discharge. A high intensity of fluorescence was observed in living T. vaginalis, epithelial cells and leukocytes present in urine and vaginal discharge. Our preliminary results show the perspective of a new diagnostic technique for trichomonosis and will contribute to the understanding of the cytoskeleton of T. vaginalis


Asunto(s)
Animales , Humanos , Femenino , Citoesqueleto , Colorantes Fluorescentes , Paclitaxel , Trichomonas vaginalis , Vaginitis por Trichomonas , Centrosoma , Flagelos , Microscopía Fluorescente , Microtúbulos , Orina , Excreción Vaginal
8.
Exp Parasitol ; 102(2): 113-6, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12706747

RESUMEN

Trichomonas vaginalis is a flagellated parasitic protist of the human urogenital tract. The parasite has a poorly known cytoskeleton formed by an axostyle and a pelta, which are formed by stable structures such as microtubules, essential for the maintenance of cell shape and organization. FLUTAX-2 is an active fluorescent derivative of Taxol, binds to alphabeta-tubulin dimer polymerized. In this paper we present the analysis of microtubule distribution in living trophozoites of T. vaginalis using FLUTAX-2.


Asunto(s)
Citoesqueleto/ultraestructura , Colorantes Fluorescentes , Paclitaxel , Paclitaxel/análogos & derivados , Taxoides , Trichomonas vaginalis/ultraestructura , Animales , Centrosoma/ultraestructura , Flagelos/ultraestructura , Colorantes Fluorescentes/química , Humanos , Microscopía Fluorescente , Microtúbulos/ultraestructura , Paclitaxel/química
9.
Rev. bras. anal. clin ; 34(3): 167-168, 2002. tab
Artículo en Portugués | LILACS | ID: lil-346058

RESUMEN

A prevalência de oocistos de Cryptosporidium parvum foi determinada em amostras fecais de 25 sidéticos de ambos os sexos com gastroenterite, durante o período de abril a maio de 2002 no Centro de Saúde Vila dos Comerciários em Porto Alegre, RS. Os oocistos foram detectados pela coloraçäo da safranina modificada a quente. Pelos dados observados das 25 amostras estudadas, 16 porcento (4) apresentaram resultados positivos e 84 porcento (21) foram negativas para a pesquisa de oocistos. No que se refere à ocorrência de oocistos de C. parvum, em relaçäo ao sexo, foi verificado que os maiores percentuais de infecçäo foram obtidos entre as pacientes do sexo feminino 12 porcento (3), enquanto que entre os sidéticos do sexo masculino o índice de infecçäo foi igual a 4 porcento (1).


Asunto(s)
Humanos , Masculino , Femenino , Cryptosporidium parvum , Heces , Infecciones por Protozoos/diagnóstico , Oocitos , Síndrome de Inmunodeficiencia Adquirida/complicaciones , Gastroenteritis , Prevalencia
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